Deafness, Aminoglycoside-Induced, also known as deafness, mitochondrial, modifier of, is related to deafness, nonsyndromic sensorineural, mitochondrial and rare genetic deafness. An important gene associated with Deafness, Aminoglycoside-Induced is TRMU (TRNA Mitochondrial 2-Thiouridylase), and among its related pathways/superpathways is Complex I biogenesis. Affiliated tissues include bone, and related phenotypes are aminoglycoside-induced hearing loss and muscle